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    ANXA9 annexin A9 [ Homo sapiens (human) ]

    Gene ID: 8416, updated on 10-Dec-2024

    Summary

    Official Symbol
    ANXA9provided by HGNC
    Official Full Name
    annexin A9provided by HGNC
    Primary source
    HGNC:HGNC:547
    See related
    Ensembl:ENSG00000143412 MIM:603319; AllianceGenome:HGNC:547
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ANX31
    Summary
    The annexins are a family of calcium-dependent phospholipid-binding proteins. Members of the annexin family contain 4 internal repeat domains, each of which includes a type II calcium-binding site. The calcium-binding sites are required for annexins to aggregate and cooperatively bind anionic phospholipids and extracellular matrix proteins. This gene encodes a divergent member of the annexin protein family in which all four homologous type II calcium-binding sites in the conserved tetrad core contain amino acid substitutions that ablate their function. However, structural analysis suggests that the conserved putative ion channel formed by the tetrad core is intact. [provided by RefSeq, Jul 2008]
    Expression
    Broad expression in kidney (RPKM 12.1), thyroid (RPKM 11.7) and 23 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See ANXA9 in Genome Data Viewer
    Location:
    1q21.3
    Exon count:
    17
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (150977306..150995634)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (150101002..150119333)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (150954768..150968110)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985204 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150903234 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150907955 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150908639 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150910911 Neighboring gene SET domain bifurcated histone lysine methyltransferase 1 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150913142 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150916657 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150922512 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150937329 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150937964 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:150945529-150946460 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 1:150946490 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1307 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1308 Neighboring gene H3K4me1 hESC enhancers GRCh37_chr1:150949461-150949964 and GRCh37_chr1:150949965-150950466 Neighboring gene uncharacterized LOC105371438 Neighboring gene ceramide synthase 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:150955292-150956153 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1700 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:150970021-150970520 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1701 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1702 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:150980776-150981318 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:150981319-150981859 Neighboring gene MINDY lysine 48 deubiquitinase 1 Neighboring gene prune exopolyphosphatase 1 Neighboring gene RNA, U6 small nuclear 884, pseudogene

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Discovery and refinement of loci associated with lipid levels.
    EBI GWAS Catalog
    Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
    EBI GWAS Catalog
    Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
    EBI GWAS Catalog
    Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
    EBI GWAS Catalog
    New loci associated with kidney function and chronic kidney disease.
    EBI GWAS Catalog

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables acetylcholine receptor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables calcium ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables calcium-dependent phospholipid binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables phosphatidylserine binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables phosphatidylserine binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables phospholipid binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in cell-cell adhesion IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in synaptic transmission, cholinergic IEA
    Inferred from Electronic Annotation
    more info
     
    Component Evidence Code Pubs
    located_in cell surface IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in synapse IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in vesicle membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    annexin A9
    Names
    annexin 31
    annexin XXXI
    annexin-9
    pemphaxin

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_003568.3NP_003559.2  annexin A9

      See identical proteins and their annotated locations for NP_003559.2

      Status: VALIDATED

      Source sequence(s)
      AJ009985, BC005830, BJ993162
      Consensus CDS
      CCDS975.2
      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
      Related
      ENSP00000357943.4, ENST00000368947.9
      Conserved Domains (1) summary
      pfam00191
      Location:117182
      Annexin; Annexin

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      150977306..150995634
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047431989.1XP_047287945.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    2. XM_047431991.1XP_047287947.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    3. XM_047431997.1XP_047287953.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    4. XM_047431999.1XP_047287955.1  annexin A9 isoform X3

    5. XM_047431983.1XP_047287939.1  annexin A9 isoform X1

    6. XM_047431984.1XP_047287940.1  annexin A9 isoform X1

    7. XM_047431986.1XP_047287942.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    8. XM_011510058.4XP_011508360.1  annexin A9 isoform X3

      Conserved Domains (1) summary
      pfam00191
      Location:117182
      Annexin; Annexin

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      150101002..150119333
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054339109.1XP_054195084.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    2. XM_054339110.1XP_054195085.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    3. XM_054339111.1XP_054195086.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6
    4. XM_054339112.1XP_054195087.1  annexin A9 isoform X3

    5. XM_054339107.1XP_054195082.1  annexin A9 isoform X1

    6. XM_054339108.1XP_054195083.1  annexin A9 isoform X2

      UniProtKB/Swiss-Prot
      O76027, Q5SZF1, Q6FI55, Q9BS00, Q9HBJ6